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32264-87-2

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32264-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32264-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,6 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 32264-87:
(7*3)+(6*2)+(5*2)+(4*6)+(3*4)+(2*8)+(1*7)=102
102 % 10 = 2
So 32264-87-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H4O/c5-4-2-1-3-4/h1-2H,3H2

32264-87-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclobut-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-Cyclobutenone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:32264-87-2 SDS

32264-87-2Relevant articles and documents

Synthesis of cyclobuteniminium salts derived from aldo-keteniminium salts and study of their reactivity in Diels-Alder reaction

Lumbroso, Alexandre,Catak, Saron,Sulzer-Mossé, Sarah,De Mesmaeker, Alain

, p. 6721 - 6725 (2014)

The synthesis of broad scope of novel monosubstituted cyclobuteniminium salts derived from aldo-keteniminium salts and acetylene or 1-propyne is described. The reactivity of cyclobuteniminium salts in Diels-Alder reactions has been studied in detail by DF

An expedient synthesis of cis/trans-1,3-disubstituted cyclobutanols

Calad, Stacie,Mans, Douglas,Morin, Justin-Alexander,O'Neill-Slawecki, Stacy,Sisko, Joseph

scheme or table, p. 4207 - 4210 (2011/09/19)

A two-step procedure is described to access 3-alkoxycyclobutanones from chloroacetyl chloride utilizing a step-wise [2+2] ketene cycloaddition followed by catalytic hydrogenation to reduce the α-chlorine in a single reaction sequence. The resulting cyclobutanones can be readily converted into a variety of cis or trans-1,3-disubstituted aminocyclobutanols and cyclobutanediols.

BISARYLCYCLOBUTENE DERIVATES AS CYCLOOXYGENASE INHIBITORS

-

, (2008/06/13)

The invention encompasses the novel compound of formula (I) useful in the treatment of cyclooxygenase-2 mediated diseases. The invention also encompasses certain pharmaceutical compositions for treatment of cyclooxygenase-2 mediated diseases comprising compounds of formula (I).

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